“CHSF has helped us so much. Thank you for everything you have done for us. It’s really helped having the extra support at a such hard time.“
Written by heart mum, Chelsea Machon
My partner Matthew and I found out that Blake had something wrong with his heart when he suddenly was really poorly on 30th September 2022.
We took him to Chesterfield Hospital to be seen and Matthew and I were told he had sepsis as well as two big infections. We were told he needed to be put on a ventilator and taken to Manchester to be in intensive care.
Once we were in Manchester, we found out Blake had a heart condition called mitral valve regurgitation. It was severe and need to be operated on.
After a week in Manchester paediatric intensive care unit, we were transferred to Leeds Children’s Hospital where Blake was seen by the cardiac surgical team straight away. They came up with a plan to operate as soon as possible which was very scary for me and Matthew.
Blake had his first open heart surgery on 13th October, and his second on 25th October to have a mechanical valve put in.
Children’s Heart Surgery Fund has helped me and Matthew so much.
They brought us toiletries when we arrived at Leeds and had nothing with us.
When we were low on funds they helped us with travel costs. This meant that our family could come up to Leeds support us when we needed it most.
Thank you for everything you have done for us. It’s really helped having this extra support at a such hard time.
It is only with your continued support that we can keep being there for more families like Chelsea, Matthew and Blake.
We can only do the work we do, because of you.
We appreciate the cost of living crisis is affecting us all, including families of the 1 in 100 babies who are born with congenital heart disease every day.
CHSF are incredibly grateful to everyone who continues to donate. If you are able to set up a regular payment to CHSF during these challenging times, we promise every penny will go towards supporting hearts for life.
MORE REAL STORIES
REAL STORIES: Cait Gregory
Heart hero Cait not only came to the open day for our forthcoming Teenage Support book (watch this space!), but has also recorded a special song in aid of CHSF. This is Cait's story in her own words. Read on! Hi, I'm Cait, and I was born with Tetralogy of Fallot. I...
REAL STORIES: Watts Family’s Spooky Sponsored Walk
When Martin and Leanne Watts were told their son had a heart defect their world was turned upside down - only to be told a year later, his baby brother had CHD too. Eight years on, both boys have had open heart surgery and the whole family want to say thank you to the...
REAL STORIES: Bella’s new INR Kit #BecauseofYou
Because of you and your amazing fundraising, CHSF are able to fund INR home testing kits for our heart warriors. These kits reduce stress and allow a patient to test their blood levels themselves at home without missing school for hospital appointments.Rebecca tells...


